Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K21/00—Fireproofing materials
  • C09K21/14—Macromolecular materials
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B82—NANOTECHNOLOGY
  • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
  • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
  • C08K3/016—Flame-proofing or flame-retarding additives
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/02—Elements
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/16—Nitrogen-containing compounds
  • C08K5/34—Heterocyclic compounds having nitrogen in the ring
  • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
  • C08K5/3477—Six-membered rings
  • C08K5/3492—Triazines
  • C08K5/34928—Salts
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
  • C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/02—Elements
  • C08K2003/026—Phosphorus
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
  • C08L61/04—Condensation polymers of aldehydes or ketones with phenols only

Definitions

• the invention relates to flame-retardant thermoplastic polymers with glow-wire resistance and to polymeric molding compositions which comprise a particular flame retardant combination.
• Polymers are often rendered flame-retardant via additions of phosphorus-containing or halogen-containing compounds.
• Red phosphorus has proven to be a particularly effective flame-retardant additive for thermoplastic polymers (Staendeke, H., Scharf, D., Kunststoffe 11, 79, 1989, and Levchik, G. F., Vorobyova, S. A., Gorbarenko, V. V., and Levchik, S., Weil, E. D., Journal of Fire Science, Vol. 18 May/June 2000, pp. 172-183).
• UL 94 V-0 classification at 0.8 mm is achieved using 7.5% of red phosphorus in reinforced and unreinforced polyamide.
• DE-A-102 24 887 describes polymers comprising a combination of red phosphorus, zinc borate, talc, and a lanthanoid compound. This combination achieves an improvement in glow-wire resistance GWFI to IEC 60695-2-12, to 960° C.
• EP-A-0 782 599 describes the action of melamine polyphosphate (MPP) as flame retardant for polymers, in particular polyamides.
• MPP melamine polyphosphate
• UL 94 V-0 classificaiton is achieved using from 25 to 30% by weight of MPP.
• US-A-2004/0021135 describes the combination of phosphinates with melamine polyphosphate. Flame retardancy is improved via the synergistic combination, as also are mechanical properties of the flame-retardant polymers.
• JP-A-10 182 940 describes flame-retardant epoxy resins with addition of melamine polyphosphate, and with phenolic-resin-encapsulated red phosphorus.
• JP-A-2001 164 063 describes polymer mixtures composed of styrene polymers and of polycarbonates or of polyesters with melamine polyphosphate and red phosphorus.
• JP-A-11 246 778 discloses flame-retardant polymers with red phosphorus and with tetrazoles, silicone powders, melamine polyphosphate, hydrated magnesium silicates, hydrated calcium borates, or vermiculite.
• JP-A-2003 041 098 describes polyesters with triazine compounds and with phosphates, phosphorus-containing triazine compounds, or encapsulated red phosphorus, and with a resin having aromatic ring structures.
• Nanocomposites are also frequently added to the abovementioned polymers.
• the nanocomposites also termed nanofillers
• DE-A-199 21 472 describes a flame-retardant polymer composition composed of polymer, magnesium hydroxide or aluminum hydroxide, and organically intercalated phyllosilicate.
• WO-A-99/29767 describes the preparation of a polyamide-nanocomposite mixture composed of nylon-6, water, and montmorillonite. Addition of the nanofiller has an advantageous effect on heat resistance. There is no description of any flame-retardant effect.
• EP-A-0 132 228 describes flame-retardant reinforced polyester molding compositions with reinforcing fillers (preferably glass fibers), flame retardants, from 0.2 to 4% by weight of an, if appropriate organically modified, phyllosilicate as antidrip agent, and from 0.05 to 2% by weight of an alkali metal salt of a monocarboxylic acid having from 6 to 22 carbon atoms.
• Flame-retardant additives described are organic halogen compounds, in particular bromine compounds or chlorine compounds, alone or with synergistically acting compounds of phosphorus or of antimony.
• red phosphorus and melamine polyphosphates are in essence assessed for fire test purposes by UL 94 vertical tests.
• the effect of the individual compounds remains unsatisfactory in specific thermoplastics.
• the effect in the IEC 60695-2-12 and -13 glow-wire test remains inadequate.
• the amounts of melamine polyphosphate which have to be added for the UL 94 test sometimes very large amounts, also cause polymer degradation and discoloration of the flame-retardant plastics, and at present this cannot be effectively countered.
• the present invention therefore provides flame-retardant polymers with glow-wire resistance, which comprise,
• component A from 40 to 90% by weight of polymer
• component B from 0 to 40% by weight of reinforcing material
• component C from 3 to 15% by weight of red phosphorus
• component D from 5 to 20% by weight of phosphorus/nitrogen flame retardant
• component E from 0 to 15% by weight of phenolic resin
• component F from 0 to 10% by weight of nanocomposites
• the flame-retardant polymers with glow-wire resistance preferably comprise amounts of from 45 to 65% by weight of component A.
• the flame-retardant polymers with glow-wire resistance particularly preferably comprise amounts of from 50 to 65% by weight of component A.
• the flame-retardant polymers with glow-wire resistance preferably comprise amounts of from 25 to 35% by weight of component B.
• the flame-retardant polymers with glow-wire resistance preferably comprise amounts of from 5 to 10% by weight of component C.
• the flame-retardant polymers with glow-wire resistance particularly preferably comprise amounts of from 7 to 10% by weight of component C.
• the flame-retardant polymers with glow-wire resistance preferably comprise amounts of from 5 to 15% by weight of component D.
• the flame-retardant polymers with glow-wire resistance particularly preferably comprise amounts of from 5 to 12% by weight of component D.
• the flame-retardant polymers with glow-wire resistance preferably comprise amounts of from 1 to 10% by weight of component E.
• the flame-retardant polymers with glow-wire resistance particularly preferably comprise amounts of from 5 to 10% by weight of component E.
• the flame-retardant polymers with glow-wire resistance preferably comprise amounts of from 1 to 5% by weight of component F.
• the flame-retardant polymers with glow-wire resistance preferably comprise amounts of from 0.05 to 10% by weight of a further component G.
• the flame-retardant polymers with glow-wire resistance particularly preferably comprise amounts of from 0.1 to 5% by weight of the further component G.
• the polymers are preferably polyamides.
• the polymers are particularly preferably reinforced polyamides.
• Preferred reinforcing materials present are glass fibers and/or mineral fillers.
• the red phosphorus present in the flame-retardant polymers with glow-wire resistance is preferably stabilized red phosphorus.
• the red phosphorus has preferably been stabilized with magnesium, tin, aluminum, silver, or a combination thereof.
• the particle size of the red phosphorus is preferably ⁇ 200 ⁇ m.
• the red phosphorus used is preferably in the form of phenolic resin concentrate.
• the phosphorus-nitrogen flame retardant is preferably reaction products of melamine with polyphosphoric acid, and/or is reaction products of condensates of melamine with polyphosphoric acid, or is a mixture of these.
• the reaction products are particularly preferably dimelamine pyrophosphate, melamine polyphosphate, melem polyphosphate, melam polyphosphate, melon polyphosphate and/or mixed polysalts of this type.
• the reaction products are in particular melamine polyphosphate.
• the nanocomposites are preferably organically intercalated phyllosilicates, nanospherical oxides, or carbon nanotubes.
• the organically intercalated phyllosilicates are preferably materials for which the starting materials are swellable smectites, such as montmorillonite, hectorite, saponite, or beidellite.
• the phyllosilicates have preferably been intercalated with quaternary ammonium compounds, with protonated amines, with organic phosphonium ions, and/or with aminocarboxylic acids.
• the reinforcing materials are preferably glass fibers, glass beads, or mineral reinforcing materials.
• the additive is preferably stabilizers, processing aids, antidrip agents, dyes, pigments, and/or waxes.
• inventive combinations of red phosphorus and phosphorus-nitrogen flame retardants such as melamine polyphosphate, and, if appropriate, of phenolic resins and nanocomposites, comply with the fire requirements of UL 94 V-0, have a GWFI of 960° C. to IEC 60695-1-12, and also have markedly improved GWIT glow-wire resistance to IEC 60695-2-13.
• inventive flame retardant combinations have good processability and give flame-retardant polymers with very good mechanical properties.
• the amount of red phosphorus (component C) used is from 3 to 15% by weight, preferably from 5 to 10% by weight, particularly preferably from 7 to 10% by weight, based on the mixing specification of the compounded material.
• the stated percentages by weight are the total proportion of phosphorus in the respective molding composition, inclusive of the stabilizers encapsulating reagents and/or phlegmatizers described above and applied to the red phosphorus.
• red phosphorus is any of the colored allotropic forms of phosphorus, preference being given to red phosphorus or types of phosphorus whose proportion of red phosphorus is greater than 95%.
• the average particle size of these particles is from 200 to 1 ⁇ m, preferably from 100 to 10 ⁇ m, particularly preferably from 80 to 20 ⁇ m.
• the red phosphorus used here may be untreated or may have been prestabilized and/or microencapsulated and/or phlegmatized with known agents.
• Phlegmatizers which may be used here are conventional reagents, such as mineral oils, paraffin oils, chloroparaffins, polytetrahydrofurans, esters of trimellitic acid, preferably of alcohols having from 6 to 13 carbon atoms, e.g. trioctyl trimellitate, and organic phosphate compounds. It is also possible to use esters of phthalic acid, which can usually be prepared from phthalic acid and from alcohols having from 6 to 13 carbon atoms. Examples of these compounds are dipentyl phthalate, dihexyl phthalate, diheptyl phthalate, dioctyl phthalate, or di-2-ethylhexyl phthalate.
• metal salt/metal compounds based inter alia on aluminum, zinc, or calcium, e.g. aluminum oxide or aluminum hydroxide, and these can also simultaneously have stabilizing effect.
• Chao, Wu et al. “A comprehensive survey of chemical dust suppressants in the world over the last 15 years”, Progress in Safety Science and Technology, Beijing, China, Aug. 10-13, 2000 (2000), (Pt. 2), 705-719 also gives an overview of phlegmatizers that can be used, supplementing the compounds listed above.
• Red phosphorus can be microencapsulated with agents known per se.
• agents known per se are polymeric compounds, such as cyclohexanone resins, melamine resins, phenol-isobutyraldehyde resins, urea-melamine-phenol-formaldehyde resins, phenol-formaldehyde resins, urea-resorcinol-formaldehyde resins, urea-resorcinol-formaldehyde-hexamethylenetetramine resins, the latter in particular prepared from a mixture of from 0.4 to 4% of urea, from 2 to 20% of resorcinol, from 5 to 150% of formaldehyde, and from 0.1 to 8% of hexamethylenetetramine, based in each case on the weight of red phosphorus used, or epoxy resins.
• polymeric compounds such as cyclohexanone resins, melamine resins, phenol-isobutyraldehy
• metal salts or metal compounds inter alia of aluminum, iron, calcium, cadmium, cobalt, nickel, magnesium, manganese, silver, tin, zinc, or titanium.
• oxides, carbonates/oxycarbonates, hydroxides, and salts of organic acids are particularly suitable here. It is also possible to use compounds such as silicon dioxide.
• the form in which the red phosphorus is introduced into the molding compositions may be either that of a powder or else that of concentrates.
• These concentrates are generally polymeric carrier materials with a proportion of from 40 to 70% by weight of phosphorus, based on the total weight of the concentrate.
• Typical polymeric carrier materials in this context are polyamides as described above, preferably nylon-6 and nylon-6,6, particularly preferably nylon-6, and the materials described above which are polyesters, epoxy resins, phenolic resins, ester waxes, LDPE or EVA. Phenolic resins are also particularly preferred.
• the phosphorus/nitrogen flame retardants (component D) are preferably reaction products of melamine with phosphoric acid or with condensed phosphoric acids, or are reaction products of condensates of melamine with phosphoric acid or with condensed phosphoric acids, or are a mixture of the products mentioned.
• the reaction products with phosphoric acid or with condensed phosphoric acids are compounds produced via reaction of melamine or of the condensed melamine compounds, such as melam, melem, or melon, etc., with phosphoric acid.
• examples of these are dimelamine phosphate, dimelamine pyrophosphate, melamine phosphate, melamine pyrophosphate, melamine polyphosphate, melam polyphosphate, melon polyphosphate, and melem polyphosphate, and mixed polysalts, e.g. those described in WO-A-98/39306.
• the phosphorus/nitrogen flame retardant is particularly preferably melamine polyphosphate.
• the nanofillers (component F) are preferably organically intercalated phyllosilicates.
• Preferred starting materials used for the organically intercalated phyllosilicates are swellable smectites, such as montmorillonite, hectorite, saponite, or beidellite.
• the layer separation of the organically intercalated phyllosilicates is from 1.5 to 4 nm.
• the phyllosilicates have preferably been intercalated with quaternary ammonium compounds, with protonated amines, with organic phosphonium ions, and/or with aminocarboxylic acids.
• the typical layer thickness of nanocomposites is smaller by a factor of from 10 to 50.
• the diameter of the fully exfoliated nanofillers varies from 100 to 500 nm, with layer thickness of only 1 nm.
• the inventive polymer comprises, as component A, from 40 to 90% by weight of polyamide; as component B, from 0 to 40% by weight of reinforcing materials, such as glass fibers, glass beads, or mineral reinforcing materials; as component C, from 3 to 15% by weight of red phosphorus; as component D, from 5 to 20% by weight of a phosphorus/nitrogen flame retardant; as component E, from 0 to 15% by weight of a phenolic resin; and optionally, as component F, from 0 to 10% by weight of a nanocomposite, where the entirety of the components always amounts to 100% by weight.
• component A from 40 to 90% by weight of polyamide
• component B from 0 to 40% by weight of reinforcing materials, such as glass fibers, glass beads, or mineral reinforcing materials
• component C from 3 to 15% by weight of red phosphorus
• component D from 5 to 20% by weight of a phosphorus/nitrogen flame retardant
• component E from 0 to 15% by weight of a phenolic resin
• the polymer comprises, as component A, from 45 to 65% by weight of polyamide; as component B, from 25 to 35% by weight of reinforcing materials, such as glass fibers, glass beads, or mineral reinforcing materials; as component C, from 5 to 10% by weight of red phosphorus; as component D, from 5 to 15% by weight of a phosphorus/nitrogen flame retardant; as component E, from 1 to 10% by weight of a phenolic resin; and as component F, from 1 to 5% by weight of a nanocomposite, where the entirety of the components always amounts to 100% by weight.
• component A from 45 to 65% by weight of polyamide
• component B from 25 to 35% by weight of reinforcing materials, such as glass fibers, glass beads, or mineral reinforcing materials
• component C from 5 to 10% by weight of red phosphorus
• component D from 5 to 15% by weight of a phosphorus/nitrogen flame retardant
• component E from 1 to 10% by weight of a phenolic resin
• component F from 1 to
• the polymer comprises, as component A, from 50 to 65% by weight of polyamide; as component B, from 25 to 35% by weight of reinforcing materials, such as glass fibers, glass beads, or mineral reinforcing materials; as component C, from 7 to 10% by weight of red phosphorus; as component D, from 5 to 12% by weight of a phosphorus/nitrogen flame retardant; as component E, from 5 to 10% by weight of a phenolic resin; and as component F, from 1 to 5% by weight of a nanocomposite, where the entirety of the components always amounts to 100% by weight.
• component A from 50 to 65% by weight of polyamide
• component B from 25 to 35% by weight of reinforcing materials, such as glass fibers, glass beads, or mineral reinforcing materials
• component C from 7 to 10% by weight of red phosphorus
• component D from 5 to 12% by weight of a phosphorus/nitrogen flame retardant
• component E from 5 to 10% by weight of a phenolic resin
• component F from
• the invention also provides a flame-retardant plastics molding composition comprising the inventive flame retardant combination.
• the plastic is preferably thermoplastic polymers or blends composed of two or more different polymers.
• thermoplastic polymers such as homo- and copolymers of olefinically unsaturated monomers, e.g. polyfluoroethylenes, polyethylene, polypropylene, ethylene-propylene copolymers, polystyrene, styrene-acrylonitrile copolymers, ABS copolymers (acrylonitrile-butadiene-styrene), vinyl chloride homo- and copolymers, polyacrylates, in particular polymethyl methacrylate, vinyl acetate copolymers, polyacetals, polycarbonates, polyesters, and polyamides. Polyamides and polyesters are preferred, and in the present context polyamides are particularly preferred.
• Suitable polyamides are known homopolyamides, copolyamides, and mixtures of these polyamides. These may be semicrystalline and/or amorphous polyamides.
• Suitable semicrystalline polyamides are nylon-6, nylon-6,6, and mixtures and appropriate copolymers composed of these components.
• Other semicrystalline polyamides which may be used are those whose acid component is composed entirely or to some extent of terephthalic acid and/or of isophthalic acid and/or of subaric acid and/or of sebacic acid and/or of azelaic acid and/or of adipic acid and/or of cyclohexanedicarboxylic acid, whose diamine component is entirely or to some extent composed of m- and/or p-xylylenediamine and/or of hexamethylenediamine and/or of 2,2,4-trimethylhexamethylenediamine and/or of 2,2,4-trimethylhexamethylenediamine and/or of isophoronediamine, and whose constitution is known in principle.
• Particularly preferred semicrystalline polyamides are nylon-6,6 and nylon-6 and their mixtures, very particular preference being given to nylon-6,6.
• Amorphous polyamides which may be used comprise known products. They are obtained via polycondensation of diamines, such as ethylenediamine, hexamethylenediamine, decamethylenediamine, 2,2,4- and/or 2,4,4-trimethylhexamethylenediamine, m- and/or p-xylylenediamine, bis(4-aminocyclohexyl)methane, bis(4-aminocyclohexyl)propane, 3,3′-dimethyl-4,4′-diaminodicyclohexylmethane, 3-aminomethyl-3,5,5-trimethylcyclohexylamine, 2,5- and/or 2,6-bis(aminomethyl)norbornane, and/or 1,4-diaminomethylcyclohexane with dicarboxylic
• Copolymers obtained via polycondensation of two or more monomers are also suitable, as are copolymers prepared with addition of aminocarboxylic acids, such as aminocaproic acid, aminoundecanoic acid, or aminolauric acid, or of their lactams.
• aminocarboxylic acids such as aminocaproic acid, aminoundecanoic acid, or aminolauric acid, or of their lactams.
• Particularly suitable amorphous polyamides are the polyamides prepared from isophthalic acid, hexamethylenediamine, and other diamines, such as 4,4′-diaminodicyclohexylmethane, isophoronediamine, 2,2,4- and/or 2,4,4-trimethylhexamethylenediamine, 2,5- and/or 2,6-bis(aminomethyl)norbornene; or from isophthalic acid, 4,4′-diaminodicyclohexylmethane and caprolactam; or from isophthalic acid, 3,3′-dimethyl-4,4′-diaminodicyclohexylmethane and laurolactam; or from terephthalic acid and the isomer mixture composed of 2,2,4- and/or 2,4,4-trimethylhexamethylenediamine.
• diamines such as 4,4′-diaminodicyclohexylmethane, isophoronedia
• Terephthalic acid can replace up to 30% of the isophthalic acid.
• Suitable reagents may also have been used to introduce branching into the polyamides described or to lengthen their polymer chains appropriately.
• Branching agents or chain extenders which may be used are low-molecular-weight and oligomeric compounds which have at least two reactive groups which can react with primary and/or secondary amino groups, and/or with amide groups, and/or with carboxylic acid groups.
• reactive groups are isocyanates, which may, if appropriate, have been capped, epoxides, maleic anhydrides, oxazolines, oxazines, oxazolones, and the like.
• diepoxides based on diglycidyl ethers bisphenol and epichlorohydrin
• amine-epoxy resin aniline and epichlorohydrin
• diglycidyl esters cycloaliphatic dicarboxylic acids and epichlorohydrin
• 2,2-bis[p-hydroxyphenyl]propane diglycidyl ether, bis[p-(N-methyl-N-2,3-epoxypropyl)aminophenyl]methane are particularly preferred, and very particular preference is given to bisphenol A diglycidyl ether.
• the polymer moldings, polymer films, polymer filaments, and polymer fibers involve HI (high-impact) polystyrene, polyphenylene ether, polyamides, polyesters, polycarbonates, and blends or polyblends of the type represented by ABS (acrylonitrile-butadiene-styrene) or PC/ABS (polycarbonate/acrylonitrile-butadiene-styrene), polyamide, or polyester, preferably polyamide.
• the abovementioned additives may be introduced into the plastic in a very wide variety of steps of the process.
• the additives may be admixed with the polymer melt at the very start of the polymerization/polycondensation process, or at its end, or in a subsequent compounding process.
• the additives are not added until later. This method is used particularly when using masterbatches of pigments or of additives. It is also possible to apply in particular pulverulent additives in a drum to the polymer pellets, which may have retained some heat from the drying process.
• the preferred form of the red phosphorus is that of a melt mixture or that of a masterbatch. Concentrates in phenolic resins are particularly preferred.
• the polyamides are preferably those of amino acid type and/or of diamine-dicarboxylic acid type.
• the polyamides are preferably nylon-6, nylon-12, semiaromatic polyamides, and/or nylon-6,6.
• the polyamides are preferably unmodified, colored, filled, unfilled, reinforced, or unreinforced polyamides, or else have been modified in some other way.
• Fibrous or particulate fillers and reinforcing materials which may be added to the inventive molding compositions are glass fibers, glass beads, glass textile, glass mats, carbon fibers, aramid fibers, potassium titanate fibers, natural fibers, amorphous silica, magnesium carbonate, barium sulfate, feldspar, mica, silicates, quartz, kaolin, titanium dioxide, wollastonite, inter alia, and these may also have been surface-treated.
• Preferred reinforcing materials are commercially available glass fibers.
• the form in which the glass fibers are added may be that of continuous-filament fibers or that of cut or ground glass fibers, the fiber diameter generally being from 8 to 18 ⁇ m, and the fibers here may, if appropriate, have been provided with surface modifications, e.g. silanes or glass-fiber sizes.
• Acicular mineral fillers are also suitable.
• acicular mineral fillers are a mineral filler with pronounced acicular character. An example which may be mentioned is acicular wollastonite.
• the L/D (length/diameter) ratio of the mineral is preferably from 8:1 to 35:1, with preference from 8:1 to 11:1.
• the mineral filler may, if appropriate, have been surface-treated.
• inventive polymers and molding compositions may comprise further additives, examples being agents to counteract decomposition caused by heat, agents to counteract crosslinking caused by heat, agents to counteract damage by ultraviolet light, plasticizers, flow aids and processing aids, further flame retardants, lubricants and mold-release agents, nucleating agents, antistatic agents, stabilizers, and dyes and pigments.
• oxidation retarders and heat stabilizers are sterically hindered phenols and/or phosphites, hydroquinones, aromatic secondary amines, such as diphenylamines, various substituted representatives of these groups, and mixtures of these.
• UV stabilizers which may be mentioned are various substituted resorcinols, salicylates, benzotriazoles, and benzophenones.
• Colorants which may be used are inorganic pigments, such as titanium dioxide, ultramarine blue, iron oxide, and carbon black, and also inorganic pigments, such as phthalocyanines, quinacridones, perylenes, and dyes, such as nigrosine and anthraquinone, and other colorants.
• inorganic pigments such as titanium dioxide, ultramarine blue, iron oxide, and carbon black
• inorganic pigments such as phthalocyanines, quinacridones, perylenes, and dyes, such as nigrosine and anthraquinone, and other colorants.
• phthalocyanines such as quinacridones, perylenes, and dyes, such as nigrosine and anthraquinone, and other colorants.
• dyes such as nigrosine and anthraquinone, and other colorants.
• carbon black it is preferable to use carbon black.
• nucleating agents examples include sodium phenylphosphinate, aluminum oxide, or silicon dioxide.
• Lubricants and mold-release agents generally used are ester waxes, pentaerythritol tetrastearate (PETS), long-chain fatty acids (e.g. stearic acid or behenic acid), the salts of these (e.g. calcium stearate or zinc stearate), and also amide derivatives (e.g. ethylenebisstearylamide), or montan waxes (mixtures of straight-chain, saturated carboxylic acids having chain lengths of from 28 to 32 carbon atoms), and low-molecular-weight polyethylene waxes and low-molecular-weight polypropylene waxes.
• PETS pentaerythritol tetrastearate
• long-chain fatty acids e.g. stearic acid or behenic acid
• the salts of these e.g. calcium stearate or zinc stearate
• amide derivatives e.g. ethylenebisstearylamide
• montan waxes mixture
• plasticizers examples which may be mentioned of plasticizers are dioctyl phthalate, dibenzyl phthalate, butyl benzyl phthalate, hydrocarbon oils, and N-(n-butyl)benzenesulfonamide.
• flame retardants examples include phosphorus-containing flame retardants selected from the groups of the mono- and oligomeric phosphoric and phosphonic esters, phosphonates, phosphinates, phosphites, hypophosphites, phosphine oxides, and phosphazenes, and the flame retardants used may also comprise mixtures of two or more components selected from one or more of these groups. It is also possible to use other, preferably halogen-free, phosphorus compounds not specifically mentioned here, alone or in any desired combination with other, preferably halogen-free, phosphorus compounds.
• Component A is a compound having Component A:
• Nylon-6,6 (PA 6.6): ®Durethan A 30 (Bayer AG, D)
• Component B ® Vetrotex EC 10 P983 Glass fibers (Vetrotex, D) ® Tremin 283 600 Wollastonite
• MPP melamine polyphosphate
• the flame retardant components were mixed in the ratio stated in the tables with the polymer pellets and, if appropriate, with the stabilizer, and incorporated in a twin-screw extruder (Leistritz ZSK 27/44) at temperatures of from 260 to 310° C. (GRPA 6.6).
• the homogenized polymer extrudate was drawn off, cooled in a water bath, and then pelletized.
• the molding compositions were processed in an injection molding machine (®Arburg 320 C Allrounder) at melt temperatures of from 270 to 320° C. (GRPA 6.6) to give test specimens, and tested and classified for flame retardancy on the basis of the UL 94 test (Underwriters Laboratories).
• the properties evaluated here are, inter alia, afterflame times and drip performance of ASTM standard test specimens.
• the classification UL 94 V-1 demands that the individual afterflame times are not longer than 30 seconds, and that the total of the afterflame times for 10 flame applications to 5 specimens is not greater than 250 seconds.
• the total afterglow time may not be more than 250 seconds.
• Classification in fire classification UL 94 V-2 applies when flaming drips are produced but the other criteria of UL 94 V-1 classification are met.
• GWFI flame retardancy of plastics in the glow-wire test
• the general procedure here uses 3 test specimens (for example plaques of dimensions 60 ⁇ 60 ⁇ 1 mm) and a glowing wire at temperatures of from 550 to 960° C. to determine, as GWFI, the maximum temperature at which an afterflame time of 30 seconds is not exceeded and the specimen does not produce any flaming drips.
• the temperature determined as GWIT is higher by 25° C. than the maximum glow-wire temperature which does not lead to ignition of the specimen (ignition meaning here that a flame is visible for longer than 5 seconds).
• test is of particular interest in the electrical and electronic sector, because the temperatures reached in electronic equipment in the event of a defect, or on overloading, are sufficiently high to cause ignition of parts in the immediate vicinity.
• the glow-wire test simulates this type of thermal stress.
• the test specimen has to have a GWFI of 850° C. and a GWIT of 775° C.
• the flowability of the molding compositions was determined via determination of the melt volume index (MVR) at 275° C./2.16 kg. A sharp rise in the MVR value indicates degradation of the polymer.
• Table 1 shows comparative examples in which red phosphorus, melamine polyphosphate (MPP), and ®Nanofil 9 were used as flame retardant.
• MPP melamine polyphosphate
• ®Nanofil 9 were used as flame retardant.
• Comparative examples (experimental series 1): flame-retardant molding compositions with the components as individual additives in ® Durethan A 30 glass-fiber-reinforced PA 6.6 with 30% of ® Vetrotex EC 10 P 983 glass fibers.
• Use of red phosphorus achieves UL 94 V-0, but not GWIT>775° C.
• Use of melamine polyphosphate likewise achieves only V-0, GWIT remaining at not more than 725° C.
• ®Nanofil achieves only V-2 and a GWIT of 650° C.
• Table 2 shows comparative examples in which the flame retardants used comprise red phosphorus combined with phenolic resin (used in the form of ®Exolit RP 689, a concentrate of 60% of red phosphorus in phenolic resin), and melamine polyphosphate (MPP) combined with ®Nanofil 9.
• phenolic resin used in the form of ®Exolit RP 689, a concentrate of 60% of red phosphorus in phenolic resin
• MPP melamine polyphosphate
• the combinations of two substances likewise achieves only a GWIT of not more than 750° C.
• Mixing specifications c12 and c13 also exhibit marked degradation of the polymer, discernible from the high MVR.
• red phosphorus alone (comparative example c14) achieves V-0, it achieves only a GWIT of from 725 to 750° C.
• the inventive combination of red phosphorus and melamine polyphosphate (ie1) achieves not only V-0 but also a GWIT of 775° C.
• phenolic resin ie2
• the MVR of ie1 to ie4 is from 17 to 23 cm 3 /10 min, and therefore the mixing specifications exhibit no degradation of the polymer.
• the inventive mixing specifications have good processability and have good mechanical and electrical properties (e.g. CTI 600V).

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